dc.contributor.author |
Estevez, Y. |
|
dc.contributor.author |
Quiliano, M. |
|
dc.contributor.author |
Burguete, A. |
|
dc.contributor.author |
Cabanillas Amado, Billy Joel |
|
dc.contributor.author |
Zimic-Peralta, Mirko Juan |
|
dc.contributor.author |
Málaga, E. |
|
dc.contributor.author |
Verastegui Pimentel, Manuela Renee |
|
dc.contributor.author |
Pérez-Silanes, S. |
|
dc.contributor.author |
Aldana, I. |
|
dc.contributor.author |
Monge, A. |
|
dc.contributor.author |
Castillo Pareja, Denis Helan |
|
dc.contributor.author |
Deharo, E. |
|
dc.date.accessioned |
2022-01-18T19:26:46Z |
|
dc.date.available |
2022-01-18T19:26:46Z |
|
dc.date.issued |
2011 |
|
dc.identifier.uri |
https://hdl.handle.net/20.500.12866/10853 |
|
dc.description.abstract |
Pyrazole and propenone quinoxaline derivatives were tested against intracellular forms of Leishmania peruviana and Trypanosoma cruzi. Both series were tested for toxicity against proliferative and non-proliferative cells. The pyrazole quinoxaline series was quite inactive against T. cruzi; however, the compound 2,6-dimethyl-3-f-quinoxaline 1,4-dioxide was found to inhibit 50% of Leishmania growth at 8.9 μM, with no impact against proliferative kidney cells and with low toxicity against THP-1 cells and murine macrophages. The compounds belonging to the propenone quinoxaline series were moderately active against T. cruzi. Among these compounds, two were particularly interesting, (2E)-1-(7-fluoro-3-methyl-quinoxalin-2-yl)-3-(3,4,5-trimethoxy-phenyl)-propenone and (2E)-3-(3,4,5-trimethoxy-phenyl)-1-(3,6,7-trimethyl-quinoxalin-2-yl)-propenone. The former possessed selective activity against proliferative cells (cancer and parasites) and was inactive against murine peritoneal macrophages; the latter was active against Leishmania and inactive against the other tested cells. Furthermore, in silico studies showed that both series respected Lipinski’s rules and that they confirmed a linear correlation between trypanocidal activities and LogP. Docking studies revealed that compounds of the second series could interact with the poly (ADP-ribose) polymerase protein of Trypanosoma cruzi. |
en_US |
dc.language.iso |
eng |
|
dc.publisher |
Elsevier |
|
dc.relation.ispartofseries |
Experimental Parasitology |
|
dc.rights |
info:eu-repo/semantics/restrictedAccess |
|
dc.rights.uri |
https://creativecommons.org/licenses/by-nc-nd/4.0/deed.es |
|
dc.subject |
Female |
en_US |
dc.subject |
article |
en_US |
dc.subject |
controlled study |
en_US |
dc.subject |
animal cell |
en_US |
dc.subject |
Animals |
en_US |
dc.subject |
Mice |
en_US |
dc.subject |
mouse |
en_US |
dc.subject |
non|priority journal |
en_US |
dc.subject |
unclassified drug |
en_US |
dc.subject |
Trypanocidal Agents |
en_US |
dc.subject |
human cell |
en_US |
dc.subject |
Trypanosoma cruzi |
en_US |
dc.subject |
Leishmania |
en_US |
dc.subject |
protozoal protein |
en_US |
dc.subject |
Leishmania peruviana |
en_US |
dc.subject |
correlation analysis |
en_US |
dc.subject |
cell proliferation |
en_US |
dc.subject |
amphotericin B |
en_US |
dc.subject |
Mice, Inbred BALB C |
en_US |
dc.subject |
Molecular Structure |
en_US |
dc.subject |
Structure-Activity Relationship |
en_US |
dc.subject |
drug synthesis |
en_US |
dc.subject |
growth inhibition |
en_US |
dc.subject |
Murinae |
en_US |
dc.subject |
antiprotozoal activity |
en_US |
dc.subject |
antitrypanosomal agent |
en_US |
dc.subject |
drug cytotoxicity |
en_US |
dc.subject |
Quinoxalines |
en_US |
dc.subject |
molecular docking |
en_US |
dc.subject |
Cercopithecus aethiops |
en_US |
dc.subject |
drug selectivity |
en_US |
dc.subject |
Vero Cells |
en_US |
dc.subject |
kidney cell |
en_US |
dc.subject |
computer model |
en_US |
dc.subject |
drug protein binding |
en_US |
dc.subject |
Macrophages, Peritoneal |
en_US |
dc.subject |
1 (7 fluoro 3 methyl quinoxalin 2 yl) 3 (3,4,5 trimethoxyphenyl)propenone |
en_US |
dc.subject |
2,6 dimethyl 3 f quinoxaline 1,4 dioxide |
en_US |
dc.subject |
3 (3,4,5 trimethoxyphenyl) 1 (3,6,7 trimethyl quinoxalin 2 yl)propenone |
en_US |
dc.subject |
mathematical computing |
en_US |
dc.subject |
nicotinamide adenine dinucleotide adenosine diphosphate ribosyltransferase |
en_US |
dc.subject |
peritoneum macrophage |
en_US |
dc.subject |
quinoxaline 1,4 oxide derivative |
en_US |
dc.subject |
Quinoxaline 1,4-di-N-oxide derivatives |
en_US |
dc.subject |
trimethoxyphenyl propenone |
en_US |
dc.subject |
trimethoxyphenyl pyrazole quinoxaline |
en_US |
dc.title |
Trypanocidal properties, structure-activity relationship and computational studies of quinoxaline 1,4-di-N-oxide derivatives |
en_US |
dc.type |
info:eu-repo/semantics/article |
|
dc.identifier.doi |
https://doi.org/10.1016/j.exppara.2011.01.009 |
|
dc.subject.ocde |
https://purl.org/pe-repo/ocde/ford#3.03.07 |
|
dc.relation.issn |
1090-2449 |
|